WO2008042422A3 - Bicyclic and tricyclic derivatives as thrombin receptor antagonists - Google Patents

Bicyclic and tricyclic derivatives as thrombin receptor antagonists Download PDF

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Publication number
WO2008042422A3
WO2008042422A3 PCT/US2007/021277 US2007021277W WO2008042422A3 WO 2008042422 A3 WO2008042422 A3 WO 2008042422A3 US 2007021277 W US2007021277 W US 2007021277W WO 2008042422 A3 WO2008042422 A3 WO 2008042422A3
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WO
WIPO (PCT)
Prior art keywords
bond
bicyclic
receptor antagonists
thrombin receptor
tricyclic derivatives
Prior art date
Application number
PCT/US2007/021277
Other languages
French (fr)
Other versions
WO2008042422A2 (en
Inventor
Samuel Chackalamannil
Mariappan V Chelliah
Yuguguang Wang
Yan Xia
Original Assignee
Schering Corp
Samuel Chackalamannil
Mariappan V Chelliah
Yuguguang Wang
Yan Xia
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
Application filed by Schering Corp, Samuel Chackalamannil, Mariappan V Chelliah, Yuguguang Wang, Yan Xia filed Critical Schering Corp
Priority to MX2009003761A priority Critical patent/MX2009003761A/en
Priority to EP07867202.9A priority patent/EP2069326B1/en
Priority to JP2009531448A priority patent/JP2010505842A/en
Priority to AU2007305269A priority patent/AU2007305269A1/en
Priority to CA002667082A priority patent/CA2667082A1/en
Publication of WO2008042422A2 publication Critical patent/WO2008042422A2/en
Publication of WO2008042422A3 publication Critical patent/WO2008042422A3/en
Priority to IL198009A priority patent/IL198009A0/en

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    • C—CHEMISTRY; METALLURGY
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/443—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

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Abstract

Heterocyclic-substituted tricyclics of the formula (I) or a pharmaceutically acceptable salt or solvate of said compound, isomer or racemic mixture wherein represents an optional double bond, the dotted line is optionally a bond or no bond, resulting in a double bond or a single bond, as permitted by the valency requirement and wherein E, A, G M, Het, B, X, R3, R10, R11, R32 and R33 are herein defined and the remaining substituents are as defined in the specification, are disclosed, as well as pharmaceutical compositions containing them and a method of treating diseases associated with thrombosis, atherosclerosis, restenosis, hypertension, angina pectoris, arrhythmia, heart failure, and cancer by administering said compounds. Combination therapy with other cardiovascular agents is also claimed.
PCT/US2007/021277 2006-10-04 2007-10-02 Bicyclic and tricyclic derivatives as thrombin receptor antagonists WO2008042422A2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
MX2009003761A MX2009003761A (en) 2006-10-04 2007-10-02 Bicyclic and tricyclic derivatives as thrombin receptor antagonists.
EP07867202.9A EP2069326B1 (en) 2006-10-04 2007-10-02 Bicyclic and tricyclic derivatives as thrombin receptor antagonists
JP2009531448A JP2010505842A (en) 2006-10-04 2007-10-02 Bicyclic and tricyclic derivatives as thrombin receptor antagonists
AU2007305269A AU2007305269A1 (en) 2006-10-04 2007-10-02 Bicyclic and tricyclic derivatives as thrombin receptor antagonists
CA002667082A CA2667082A1 (en) 2006-10-04 2007-10-02 Bicyclic and tricyclic derivatives as thrombin receptor antagonists
IL198009A IL198009A0 (en) 2006-10-04 2009-04-05 Bicyclic and tricyclic derivatives as thrombin receptor antagonists

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US84935406P 2006-10-04 2006-10-04
US60/849,354 2006-10-04

Publications (2)

Publication Number Publication Date
WO2008042422A2 WO2008042422A2 (en) 2008-04-10
WO2008042422A3 true WO2008042422A3 (en) 2009-03-26

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2007/021277 WO2008042422A2 (en) 2006-10-04 2007-10-02 Bicyclic and tricyclic derivatives as thrombin receptor antagonists

Country Status (13)

Country Link
US (2) US8153664B2 (en)
EP (1) EP2069326B1 (en)
JP (1) JP2010505842A (en)
KR (1) KR20090074219A (en)
CN (1) CN101541782A (en)
AR (1) AR063123A1 (en)
AU (1) AU2007305269A1 (en)
CA (1) CA2667082A1 (en)
IL (1) IL198009A0 (en)
MX (1) MX2009003761A (en)
TW (1) TW200823205A (en)
WO (1) WO2008042422A2 (en)
ZA (1) ZA200902362B (en)

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JP5512534B2 (en) * 2007-12-07 2014-06-04 アンセルム（アンスチチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル） Methods for treatment and diagnosis of bone mineral density related disorders
PT2438060E (en) * 2009-06-04 2013-12-16 Merck Sharp & Dohme Active metabolite of a thrombin receptor antagonist
NZ600008A (en) 2009-12-04 2014-10-31 Sunovion Pharmaceuticals Inc Multicyclic compounds and methods of use thereof
WO2011128421A1 (en) 2010-04-16 2011-10-20 Sanofi Tricyclic pyridyl-vinyl pyrroles as par1 inhibitors
PL2558462T3 (en) 2010-04-16 2015-03-31 Sanofi Sa Pyridyl-vinyl-pyrazolo-chinolines as PAR1 inhibitors
WO2013134012A1 (en) 2012-03-06 2013-09-12 Merck Sharp & Dohme Corp. Preparation and use of bicyclic himbacine derivatives as par-receptor antagonists
WO2015026685A1 (en) 2013-08-22 2015-02-26 Merck Sharp & Dohme Corp. 7a-heterocycle substituted- 6, 6-difluoro bicyclic himbacine derivatives
US9701669B2 (en) 2013-08-22 2017-07-11 Merck Sharp & Dohme Corp. Preparation and use of 7a-amide substituted- 6,6-difluoro bicyclic himbacine derivatives as PAR-1 receptor antagonists
US9808473B2 (en) 2013-08-22 2017-11-07 Merck Sharp & Dohme Corp. Preparation and use of 3-pyridyl substituted-6,6-difluoro bicyclic himbacine derivatives as par-1 receptor antagonists
WO2016060940A1 (en) * 2014-10-15 2016-04-21 Merck Sharp & Dohme Corp. Preparation and use of cyclic sulfonamide derivatives as par-1 receptor antagonists
WO2016058144A1 (en) * 2014-10-15 2016-04-21 Merck Sharp & Dohme Corp. Preparation and use of cyclic sulfonamide derivatives as par-1 receptor antagonists
CN105985303B (en) * 2015-02-13 2020-08-14 上海彩迩文生化科技有限公司 Preparation method of anticoagulant, intermediate and preparation method thereof
CN105732595B (en) * 2015-12-22 2018-08-28 山东大学 PAR-1 inhibitor based on terpene derivant and preparation method thereof and the purposes in treating thrombotic diseases
CN107129477A (en) * 2016-02-26 2017-09-05 上海星泰医药科技有限公司 The preparation method of (dihydronaphthalene [the 2,3-c] -6- furyls of (1R, 3aR, 4aR, 6R, 8aR, 9S, 9aR) -9- formoxyl -1- methyl -3- oxa-s ten) carboxylic acid, ethyl ester
BR112019001407A2 (en) 2016-07-29 2019-07-09 Pgi Drug Discovery Llc compounds and compositions and uses thereof
US10196403B2 (en) 2016-07-29 2019-02-05 Sunovion Pharmaceuticals Inc. Compounds and compositions and uses thereof
CA3053903A1 (en) 2017-02-16 2018-08-23 Sunovion Pharmaceuticals Inc. Methods of treating schizophrenia
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CN110627710B (en) * 2019-09-29 2020-06-05 山东大学 Novel PAR-1 inhibitor, preparation method thereof and application thereof in preventing and/or treating thrombotic diseases
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US6063847A (en) * 1997-11-25 2000-05-16 Schering Corporation Thrombin receptor antagonists
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